| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.149814922C>T | CA12012722 | PPARGC1B | c.79-5511C>T (n.79-5511C>T) c.4-5511C>T (n.4-5511C>T) n.433-2691C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.149814922C>G | CA1590664605 | PPARGC1B | c.79-5511C>G (n.79-5511C>G) c.4-5511C>G (n.4-5511C>G) n.433-2691C>G | dbSNP |